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Sustained embryoid body formation and culture in a non-laborious three dimensional culture system for human embryonic stem cells

机译:在人类胚胎干细胞的非劳动三维培养系统中持续的拟胚体形成和培养

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摘要

Pluripotent human embryonic stem cell (hESC) lines are a promising model system in developmental and tissue regeneration research. Differentiation of hESCs towards the three germ layers and finally tissue specific cell types is often performed through the formation of embryoid bodies (EBs) in suspension or hanging droplet culture systems. However, these systems are inefficient regarding embryoid body (EB) formation, structural support to the EB and long term differentiation capacity. The present study investigates if agarose, as a semi solid matrix, can facilitate EB formation and support differentiation of hESC lines. The results showed that agarose culture is able to enhance EB formation efficiency with 10% and increase EB growth by 300%. The agarose culture system was able to maintain expression of the three germ layers over 8 weeks of culture. All of the four hESC lines tested developed EBs in the agarose system although with a histological heterogeneity between cell lines as well as within cell lines. In conclusion, a 3-D agarose culture of spherical hESC colonies improves EB formation and growth in a cost effective, stable and non-laborious technique.
机译:多能人类胚胎干细胞(hESC)系是发展和组织再生研究中有希望的模型系统。 hESCs向三个胚层的分化以及最终组织特异性细胞类型的分化通常是通过在悬浮或悬浮液滴培养系统中形成胚状体(EBs)来进行的。但是,这些系统在胚状体(EB)的形成,对EB的结构支持以及长期分化能力方面效率不高。本研究调查了琼脂糖作为半固体基质是否可以促进EB的形成并支持hESC系的分化。结果表明,琼脂糖培养能够提高EB形成效率10%,并使EB生长增加300%。琼脂糖培养系统能够在培养的8周内维持三个胚层的表达。测试的所有四个hESC系均在琼脂糖系统中发育出EB,尽管在细胞系之间以及在细胞系内均具有组织学异质性。总之,球形hESC菌落的3-D琼脂糖培养物以经济有效,稳定且不费力的技术改善了EB的形成和生长。

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